戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 430460作成日:2026年10月26日

Ethyl Acetate → Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoate

https://huagongshe.com/reaction/430460

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Ammonium ChlorideHCID 25517—
反応物3-Bromo-2-methyl-1-propeneHCID 357785—
反応物Ethyl 3,3,3-trifluoro-2-oxopropanoateHCID 2737239—
触媒ManganeseHCID 23930—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoateHCID 17935595—

反応条件

温度0 °C

反応手順

1.3 g of anhydrous zinc chloride and 13.2 g of granular manganese are heated to boiling in 100 ml of tetrahydrofuran and boiled with 0.2 ml of methallyl bromide for 30 minutes. Then, the solution of 25 g of methallylbromide and 17 g of trifluoropyruvic acid ethyl ester in 80 ml of tetrahydrofuran is added in drops at boiling heat over two hours and boiled for another hour. Then, it is added to saturated ammonium chloride solution and 300 ml of ethyl acetate while being cooled with ice, stirred for 30 minutes at 0° C., and the separated ethyl acetate phase is washed with saturated ammonium chloride solution and three times with water. The solvent is dried (Na2SO4) and concentrated by evaporation, and the residue is distilled in a vacuum. 17.6 g of 2-hydroxy-4-methylene-2-trifluoromethyl-valeric acid ethyl ester, boiling point 48° C., 1 hPa, is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323199B1
出典データセットuspto-grants-2001_11
ORD IDord-605ea9751b734934af7fb3bb1d09a996
出典メモuspto-grants-2001_11